Use of Lipid Composition and Metabolism to Examine Structure and Activity of Estuarine Detrital Microflora

Author:

King John D.1,White David C.1,Taylor Cecile W.1

Affiliation:

1. Department of Biological Science, Florida State University, Tallahassee, Florida 32306

Abstract

Earlier studies have shown that the activity of the estuarine detrital microflora measured by various enzyme activities, muramic acid and adenosine 5′-triphosphate (ATP) content, heterotrophic potentials, and respiratory activities correlates with the incorporation of 14 C and 32 P into the microbial lipids. In this study, these lipids were reproducibly fractionated into neutral lipid, glycolipid, and phospholipid classes. Distinct differences between the active microflora of oak leaves, sweet gum leaves, and pine needles were evidenced both in the rate of lipid synthesis and in the proportions of neutral lipids, glycolipids, and phospholipids. Successional changes in the microflora of leaves incubated in a semitropical estuary, previously suggested by ATP-to-muramic acid ratios and scanning electron micrography, were reflected in changes in the proportions of 14 C in major lipid classes when analyzed from the same type of detritus. Short incubation times with 14 C gave lipid compositions rich in phospholipids that are typical for the faster-growing bacterial populations; longer incubation with 14 C gave lipid compositions richer in neutral and glycolipids, more characteristic of slower-growing eukaryotes or morphologically more complex prokaryotes. The metabolism of the lipids of the estuarine detrital microflora was examined by a pulse-chase experiment with 14 C. Glycolipids lost 14 C at a rate equal to the loss of 14 C of the slow component of muramic acid. Individual phospholipids lost 14 C from their backbone glycerol esters at different rates.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference29 articles.

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3. The use of the ATP assay in terrestrial decomposition studies;Ausmus B. S.;Bull. Ecol. Res. Comm.,1973

4. A rapid method of total lipid extraction and purification;Bligh E. G.;Can. J. Biochem. Physiol.,1959

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